Landscape approaches to the analysis of aquatic ecosystems

1. In the mid-1970s, Hynes (1975) wrote eloquently about the complex interactions between aquatic and terrestrial systems. Central theories in stream ecology developed thereafter have dealt with the longitudinal flow of energy, materials and organisms in streams, and, with the exception of the flood pulse concept (Junk, Bayley & Sparks, 1989), have largely ignored areas outside the riparian zone. The structure of the upland and activities occurring there play a more important part than previously recognized in regulating community structure and ecosystem processes in streams.
2. These new perspectives are made possible by developments in hierarchy theory, patch dynamics, and the refinement of tools used to quantify spatial and temporal heterogeneity.
3. Geographical information systems (GIS), image processing technology and spatial statistical techniques allow quantitative assessment of lateral, longitudinal and vertical components of the landscape that interact at several spatial and temporal scales to influence streams. When GIS is used in concert with geostatistics, multivariate statistics, or landscape models, complex relationships can be elucidated and predicted.
4. To a certain extent, the tools discussed above have only automated functions that were previously performed manually. This suite of tools has improved the ability of aquatic ecologists to examine relationships and test theories over larger, more heterogeneous regions than were previously possible.
5. At the local, state and federal level, management and regulatory frameworks are currently being re-evaluated to incorporate this new perspective in resource management and policy decision making.
6. We will discuss current and future trends in technologies and tools used for aquatic ecosystem research, and the use of techniques as they are applied in these regional assessments are also discussed.     

Re-mating between and within breeding seasons in the Greater Flamingo Phoenicopterus ruber roseus

Data on re-mating between and within breeding seasons were collected between 1983 and 1994 as part of a long-term study of the Greater Flamingo Phoenicopterus ruber roseus in the Camargue, southern France. Flamingos have bred in the Rhône delta for centuries and since 1972 have done so annually on an artificial island in the Etang du Fangassier. A sample of chicks has been ringed each year since 1977; many of these birds were later observed back at the breeding site and were used in this study. The mate-switching rate between consecutive breeding seasons was 98.3%. This result is contrary to what has been reported from captive flocks where extensive mate fidelity occurred between consecutive breeding seasons. Mate-switching also was observed in the Camargue within breeding seasons, following breeding failure, and seems to be linked to male breeding strategy in response to the need to synchronize hatching and the limited energy supply of breeding females. The absence of a long-term pair bond in Greater Flamingos contrasts with current views on the evolution of mate fidelity in relation to longevity in birds.     

Mitochondria transfer into mouse ova by microinjection

A method for mitochondria isolation and interspecific transfer of mitochondria was developed in mice. Mitochondria were isolated from Mus spretus liver samples for microinjection into fertilized ova obtained from superovulated M. musculus domesticus females. Electron microscopic observations of mitochondria preparations used for microinjection demonstrated intact mitochondrial vesicles with little microsomal contamination. Species-specific nested PCR primers complementary to sequence differences in the mitochondrial DNA D-loop region revealed high rates of successful transfer of foreign mitochondria after isolation and injection into zygotes cultured through the blastocyst stage of embryonic development. Of 217 zygotes, 67 survived mitochondria injection and 23 out of 37 zygotes developed were at the blastocyst-stage of embryonic development after 4.5 days of in vitro culture. All 23 of these blastocysts contained detectable levels of foreign mitochondria. These results represent an initial step in developing a model system to study mitochondrial dynamics and development of therapeutic strategies for human metabolic diseases affected by aberrations in mitochondrial function or mutation     

Sites of acid phosphatase in the differentiating root protophloem of Nymphoides peltata (S.G. Gmel.) O. Kuntze.

Abstract Sites of acid-phosphatase activity were found in the differentiating root protophloem of Nymphoides peltata by lead-salt and by azo-dye methods. Different substrates revealed different subcellular locations of the enzyme. The substrates β-glycerophosphate (β-GP) and naphthol ASBI phosphate revealed enzyme activity at similar sites within the sieve element. These sites included plasmodesmata, dictyosomes and small vacuoles in the cytoplasm. The substrate p-nitrophenylphosphate (p-NPP), however, revealed additional sites of acid-phosphatase activity which were not detectable by either naphthol ASBI phosphate or β-GP. For example, the inner region of the wall in mature sieve elements showed conspicuous acid-phosphatase activity only when p-NPP was used as substrate. The significance of the different locations of acid phosphatase within the sieve element is discussed. The convoluted ER, characteristic of immature sieve elements of N. peltata, failed to show acid-phosphatase activity whichever substate was used. By contrast, the stacked ER found in the parietal layer of mature sieve elements showed prominent acid-phosphatase activity regardless of the substrate used. The demonstration of acid-phosphatase activity in the stacked ER, and by both lead-salt and azo-dye methods, suggests that this organelle is a true site of acid-phosphatase activity. The onset of acid-phosphatase activity in the ER in later stages of sieve-element differentiation is compatible with the view that stacked ER plays a role in the final autolysis of the sieve-element protoplast.